Cite
Parental mosaic cutaneous-gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis-deafness syndrome.
MLA
Cohen-Barak, Eran, et al. “Parental Mosaic Cutaneous-Gonadal GJB2 Mutation: From Epidermal Nevus to Inherited Ichthyosis-Deafness Syndrome.” The Journal of Dermatology, vol. 49, no. 3, Mar. 2022, pp. 379–82. EBSCOhost, https://doi.org/10.1111/1346-8138.16268.
APA
Cohen-Barak, E., Mwassi, B., Zagairy, F., Danial-Farran, N., Khayat, M., Tatour, Y., & Ziv, M. (2022). Parental mosaic cutaneous-gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis-deafness syndrome. The Journal of Dermatology, 49(3), 379–382. https://doi.org/10.1111/1346-8138.16268
Chicago
Cohen-Barak, Eran, Bannan Mwassi, Fadia Zagairy, Nada Danial-Farran, Morad Khayat, Yasmin Tatour, and Michael Ziv. 2022. “Parental Mosaic Cutaneous-Gonadal GJB2 Mutation: From Epidermal Nevus to Inherited Ichthyosis-Deafness Syndrome.” The Journal of Dermatology 49 (3): 379–82. doi:10.1111/1346-8138.16268.